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    Resources

    Ethylene Oxide

    Why is the sterility of your drug product much more than just a test of sterility?

    A lack of sterility and sterility assurance continue to be a significant reason for drug recalls and regulatory citations and...

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    Key Elements of a Sterility Assurance Program

    This presentation will provide aspects of a sterility assurance program for a pharmaceutical product. Sterility assurance begins at the early…

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    The Road to Parametric Release for EO Sterilization

    This technical presentation and industry Q&A will define parametric release, review the advantages that merit its consideration, and provide a practical way to implement the process.

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    Process Definition – The Critical First Steps in the Validation of an EO Sterilization Process

    In this course, you will learn about the importance of process definition (fractional) work as a part of an EO validation and why it is not only important but required.

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    Best Practice Implementation of Parametric Release for EO Sterilization

    This presentation will describe the benefits of parametric release and how best to establish a compliant and capable process design.

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